HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyridine → 2-Pyridinamine, N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | 3-(3-(Piperidin-1-ylmethyl)phenoxy)propan-1-amine | HCID 10220561 | — |
| Solvent | Chloroform methanol | HCID 21584188 | — |
| Product | 2-Pyridinamine, N-[3-[3-(1-piperidinylmethyl)phenoxy]propyl]- | HCID 10019237 | — |
Reaction Steps
3-[3-(Piperidinomethyl)phenoxy]propylamine (20 g) and 2-bromopyridine (12.64 g) were stirred at 125° C. for 31/2 days. The cooled reaction mixture was subjected to column chromatography on silica ((chloroform:methanol 10:1) to afford the title compound as an oil. This was treated with maleic acid in ethanol to give, on addition of diethyl ether, as a white solid 2-[3-[3-(piperidinomethyl)phenoxy]propylamino]pyridine dimaleate (11.40 g), m.p. 116°-167° C. (recrystallised from isopropanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04681883 |
| Source dataset | uspto-grants-1987_07 |
| ORD ID | ord-9a72b13f96694b2285d86f3f0c3e2272 |
| Source note | uspto-grants-1987_07 |